Immobilized boronic acid for Suzuki–Miyaura coupling: application to the generation of pharmacologically relevant molecules
| dc.citation.title | RSC Advances | es |
| dc.citation.volume | (56) | es |
| dc.creator | Martínez-Amezaga, Maitena | |
| dc.creator | Delpiccolo, Carina M. L. | |
| dc.creator | Mata, Ernesto Gabino | |
| dc.date.accessioned | 2020-12-23T21:08:19Z | |
| dc.date.available | 2020-12-23T21:08:19Z | |
| dc.date.issued | 2017-07-12 | |
| dc.description | An synthetic strategy for the generation of a variety of biaryl and related derivatives, based on Suzuki– Miyaura coupling using immobilized boronic acid, is described. The importance of the methodology was demonstrated by its further application to biologically interesting compounds such as 4-biaryl-blactams, descripted as cholesterol absorption inhibitors and anti-MRSA active agents, neoflavonoids, imidazoles, isoxazolines, among others. | es |
| dc.description | This is a post-peer-review, pre-copyedit version of an article published in RSC Advances. The final authenticated version is available online at: https://doi.org/10.1039/c7ra06662g | |
| dc.description.fil | Fil: Martínez-Amezaga, Maitena. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR -CONICET); Argentina. | es |
| dc.description.fil | Fil: Delpiccolo, Carina M. L. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR -CONICET); Argentina. | es |
| dc.description.fil | Fil: Mata, Ernesto Gabino. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR -CONICET); Argentina. | es |
| dc.description.sponsorship | Agencia Nacional de Promoción Científica y Tecnológica (ANPCyT) | es |
| dc.description.sponsorship | Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) | es |
| dc.format | application/pdf | |
| dc.format.extent | 34994–35003 | es |
| dc.identifier.issn | 2046-2069 | es |
| dc.identifier.uri | http://hdl.handle.net/2133/19545 | |
| dc.language.iso | eng | es |
| dc.publisher | Royal Society of Chemistry | es |
| dc.relation.publisherversion | https://doi.org/10.1039/c7ra06662g | es |
| dc.relation.publisherversion | https://pubs.rsc.org/en/content/articlelanding/2017/RA/C7RA06662G#!divAbstract | es |
| dc.rights | openAccess | es |
| dc.rights.holder | Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas | es |
| dc.rights.holder | Royal Society of Chemistry | es |
| dc.rights.holder | Martínez-Amezaga, Maitena | es |
| dc.rights.holder | Delpiccolo, Carina M. L. | es |
| dc.rights.holder | Mata, Ernesto Gabino | es |
| dc.rights.text | Attribution 3.0 Unported (CC BY 3.0) | es |
| dc.rights.uri | https://creativecommons.org/licenses/by/3.0/ | * |
| dc.subject | Boronic Acids | es |
| dc.subject | Suzuki–Miyaura Coupling | es |
| dc.subject | Solid-Phase Organic Synthesis | es |
| dc.title | Immobilized boronic acid for Suzuki–Miyaura coupling: application to the generation of pharmacologically relevant molecules | es |
| dc.type | article | |
| dc.type | artículo | |
| dc.type | publishedVersion | |
| dc.type.collection | articulo | |
| dc.type.version | publishedVersion | es |